1. Meckel JF: Beschreibung Zweier durch sehr qehnliche Bildungsabweichungen entstellter Geschwister. Dtsch Arch Physiol1822;7:99-99.
2.
2. Salonen R, Norio R: The Meckel syndrome in Finland: Epidemiologic and genetic aspects. Am J Med Genet1984;18:691-698.
3.
3. Opitz J, Howe J: The Meckel syndrome (dysencephalia splanchnocystica, the Gruber syndrome). Birth Defects1969;5:167-179.
4.
4. Mecke J, Passarge E: Encephalocele, polycystic kidneys and polydactyly as an autosomal recessive trait simulating certain other disorders. Ann Genet (Paris)1971;14:97-97.
5.
5. Aleksic S, Budzilofich G, Greco MA, et al: Cerebellocele and associated central nervous system anomalies in the Meckel syndrome. Child's Brain1984;11:99-111.
6.
6. Shapiro L, Kaback M, Toomey K, Sarti D, Luther P, Cousins L: Prenatal diagnosis of the Meckel syndrome: Use of serial ultrasound and alpha-fetoprotein measurements. Birth Defects1977;8:267-272.
7.
7. Nevin N, Thompson G, Davidson G, et al: Prenatal diagnosis of the Meckel syndrome. Clin Genet1979;15:1-4.
8.
8. Karjalainen O, Aula P. Seppdla M, Hartikainen-Sorri A, Ryyndnen M: Prenatal diagnosis of the Meckel syndrome. Obstet Gynecol1981;57(suppl 6):13-15.
9.
9. Chemke J, Miskin A, Rav-Acha Z: Prenatal diagnosis of Meckel syndrome alpha fetoprotein and beta-trace protein in amniotic fluid. Clin Genet1977;11:285-289.
10.
10. Meizner I, Maor E, Katz M, Bar-David E: Prenatal early sonographic diagnosis of Meckel syndrome. Isr J Med Sci1987;23:902-904.
11.
11. Aula P. Karjalainen O, Rapola J, Lindgren J, Seppdli M: Prenatal diagnosis of Meckel syndrome. Am J Obstet Gynecol1977;129:700-702.
12.
12. Kaffe S, Godmilow I, Walker B, et al: Prenatal diagnosis of bilateral renal agenesis. Obstet Gynecol1977;49:478-480.
13.
13. Miskin M, Rudd N, Dische M, Benzie R, Pirani B: Prenatal ultrasonic diagnosis of occipital encephalocele. Am J Obstet Gynecol1978;130:585-587.
14.
14. Seller MJ: Meckel syndrome and the prenatal diagnosis of neural tube defects. J Med Genet1978;15:462-465.
15.
15. Fisher C, Warren P: Early diagnosis of Meckel's syndrome. Aust NZ J Obstet Gynaecol1980;20:53-53.
16.
16. Wapner R, Kurtz A, Ross R, Jackson L: Ultrasonographic parameters in the prenatal diagnosis of Meckel syndrome. Obstet Gynecol1981;57:388-392.
17.
17. Leucht W, Heyes H, Muiller E, Schmidt W: The Meckel syndrome (author's translation). Geburtshilfe Fraunheilkd1981;41:765-768.
19. Schmidt W, Kubli F: Early diagnosis of severe congenital malformations by ultrasonography. J Perinat Med1982;10:233-241.
20.
20. Pardes J, Engel I, Blomquist K, et al: Ultrasonography of intrauterine Meckel's syndrome. J Ultrasound Med1984;3:33-35.
21.
21. Muhlhaus K, Schneider J: Prenatal diagnosis of Meckel-Gruber syndrome (author's translation). Z Geburtshilfe Perinatol1985;189:37-41.
22.
22. Degenhardt F, Mulhaus K: Prenatal diagnosis of Meckel's syndrome in a family (author's translation). Ultraschall Med1985;6:226-228.
23.
23. Gembruch V, Hansmann M: Artificial instillation of amniotic fluid as a new technique for the diagnostic evaluation of cases of oligohydramnios. Prenat Diagn1988;8:33-45.
24.
24. Meckel S, Passage E: Encephalocele, polycystic kidneys and polydactyly as an autosomal recessive trait simulating certain other disorders: The Meckel syndrome. Ann Genet (Paris)1971;14:97-101.
25.
25. Moerman P. Verbeken E, Fryzns JP, et al: The Meckel syndrome: Pathological and cytogenetic observations in eight cases. Hum Genet1982;62:240-245.
26.
26. Bernstin J, Brough AJ, McAdams AJ: The renal lesions in syndromes of multiple congenital malformations. Birth Defects1974;10:35-43.
27.
27. Jeanty P. Romero R, d'Alton M, et al: In utero sonographic detection of hand and foot deformities. J Ultrasound Med1985;4:595-601.
28.
28. Zerres K, Hansmann M, Mallmann R: Autosomal recessive polycystic kidney disease: Problems of prenatal diagnosis. Prenat Diagn1988;8:215-229.